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WO2008033001A1 - Bactéries coryneformes présentant une productivité de l-lysine améliorée et procédé de production de l-lysine associé - Google Patents

Bactéries coryneformes présentant une productivité de l-lysine améliorée et procédé de production de l-lysine associé Download PDF

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WO2008033001A1
WO2008033001A1 PCT/KR2007/004478 KR2007004478W WO2008033001A1 WO 2008033001 A1 WO2008033001 A1 WO 2008033001A1 KR 2007004478 W KR2007004478 W KR 2007004478W WO 2008033001 A1 WO2008033001 A1 WO 2008033001A1
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Prior art keywords
gene
microorganism
lysine
set forth
corynebacteria
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English (en)
Inventor
Young Hoon Park
Sang Jo Lim
Jun Ok Moon
So Yeon Rah
Hee Jong Lee
Jae Woo Jang
Do Hyun Kwon
Hyo Jin Kim
Jin Suck Sung
Hyung Joon Kim
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CJ Corp
CJ CheilJedang Corp
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CJ Corp
CJ CheilJedang Corp
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Priority to BRPI0716980-9A2A priority Critical patent/BRPI0716980A2/pt
Priority to JP2009528183A priority patent/JP5756259B2/ja
Priority to EP07808268A priority patent/EP2066782A4/fr
Priority to CN2007800341803A priority patent/CN101573438B/zh
Priority to AU2007295159A priority patent/AU2007295159B2/en
Priority to US12/441,358 priority patent/US9109242B2/en
Publication of WO2008033001A1 publication Critical patent/WO2008033001A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20—Bacteria; Culture media therefor
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • C12P13/08—Lysine; Diaminopimelic acid; Threonine; Valine
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004—Oxidoreductases (1.)
    • C12N9/001—Oxidoreductases (1.) acting on the CH-CH group of donors (1.3)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10—Transferases (2.)
    • C12N9/1096—Transferases (2.) transferring nitrogenous groups (2.6)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10—Transferases (2.)
    • C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
    • C12N9/1217—Phosphotransferases with a carboxyl group as acceptor (2.7.2)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88—Lyases (4.)

Definitions

  • the present invention relates to a variant of Corynebacterium which shows activity greater than the endogenous activity of aspartate aminotransferase, aspartate kinase, aspartate semialdehyde dehydrogenase, dihydrodipicolinate synthase, dihydrop- icolinate reductase and diaminopimelate dicarboxylase and additionally pyruvate carboxylase, and a method of producing L- lysine using the same.
  • Corynebacterium especially, Corynebacterium glutamicum, is a Gram-positive microorganism which is widely used in the production of L-amino acids.
  • L-amino acids L-lysine is applicable in a variety of industries, including animal feedstuff, pharmaceutical and cosmetic industries. For use in these industries, typically, L-lysine is produced by fermentation using Corynebacterium strains.
  • Corynebacterium strains anchoring enhanced genes involved in lysine biosynthesis and methods of producing L-lysine are well known in the art.
  • U.S. Pat. No. 6,746,855 discloses corynebacteria strains with an enhanced lysE gene (lysine export carrier gene), to which genes selected from the group comprising a dap A gene, a lysC gene, a pyc gene and a dapB gene are additionally introduced, and a method for the production of L-lysine by cultivating the strains.
  • lysE gene lysine export carrier gene
  • 6,221,636 discloses a coryneform bacterium carrying a recombinant DNA comprising a DNA sequence coding for aspartokinase, in which the feedback inhibitory activity of L-lysine and L- threonine is substantially desensitized, and a DNA sequence coding for a diaminopimelate decarboxylase.
  • Corynebacterium spp. which show higher activity of the six enzymes involved in the biosynthesis pathway of lysine, that is, aspartate aminotransferase, aspartate kinase, aspartate semialdehyde dehydrogenase, dihydrodipicolinate synthase, dihydropicolinate reductase, and diaminopimelate dicarboxylase, than the endogenous activity thereof, mentioned in any document published prior to the present invention. Furthermore, Corynebacterium spp. that show more than the endogenous activity of pyruvate carboxylase in addition to the six enzymes are not found in any documents published prior to the present invention. Disclosure of Invention Technical Problem
  • the present invention provides a strain of
  • Corynebacteria anchoring aspartate aminotransferase, aspartate kinase, aspartate semialdehyde dehydrogenase, dihydrodipicolinate synthase, dihydropicolinate reductase and diaminopimelate dicarboxylase which show higher than their respective endogenous activities.
  • Corynebacteria in which the activity of pyruvate carboxylase is higher than the endogenous activity thereof, in addition to the six enzymes.
  • the Corynebacteria strains of the present invention show activities of the seven enzymes at higher levels than their endogenous levels.
  • the elevated enzyme activity in accordance with the present invention is based on various factors including an increase in the number of gene copies, the replacement of native promoters with more potent promoters, and artificial mutation directed to activity enhancement.
  • the number of gene copies can be increased by the introduction of an exogenous allele and/or by the amplification of the endogenous gene.
  • substitution of the gene promoter examples thereof include the introduction of an exogenous promoter having potent activity to express the structural genes downstream thereof and replacement with an endogenous gene promoter.
  • Gene amplification may be readily achieved using a method well known in the art, for example, by culturing under suitable conditions.
  • the Coryneform bacteria of the present invention features the presence of at least one copy of aspB (a gene encoding aspartate aminotransferase), lysC (a gene encoding aspartate kinase), asd (a gene encoding aspartate semialdehyde dehydrogenase), dap A (a gene encoding dihy- drodipicolinate synthase), dapB (a gene encoding dihydrodipicolinate reductase) and lysA (a gene encoding diaminopimelate dicarboxylate) in addition to the endogenous genes aspB, lysC, asd, dap A, dapB and lysA in the nuclear DNA thereof.
  • potent exogenous promoters may be located upstream of the initiation codon of the respective structural genes.
  • the coryneform bacteria of the present invention feature the presence of at least one copy of a pyc (pyruvate carboxylase) gene in addition to the endogenous pyc gene in the nuclear DNA thereof, with at least one copy of aspB, lysC, asd, dap A, dapB and lysA located therein.
  • a potent exogenous promoter is located upstream of the initiation codon of the pyc gene while potent exogenous promoters replace endogenous promoters of the six respective genes.
  • Corynebacterium any coryneform bacteria can be used as a mother strain into which the genes are introduced.
  • Corynebacterium microorganisms useful in the present invention include Corynebacterium glutamicum ATCC 13032, Corynebacterium glutamicum, Corynebacterium thermoaminogenes FERM BP- 1539, Brevibacterium flavumATCC 14067, Brevibacterium lactofermentum ATCC 13869, and L- amino acid-producing mutants or strains derived therefrom, such as Corynebacterium glutamicum KFCC1O881 and Corynebacterium glutamicum KFCCI lOOl, with preference for Corynebacterium glutamicum KFCC 10881.
  • aspB, lysC, asd, dapA, dapB, lysA and pyc have nucleotide sequences of SEQ ID NOS.: 25, 26, 27, 28, 29, 30 and 37, respectively, each comprising a native promoter and a termination codon.
  • the Corynebacteria microorganisms of the present invention may be coryneform bacteria into which vectors pDZ-2aspB, pDZ-21ysC/asd, pDZ-2dapA/dapB, pDZ- 21ysA and pDZ-2pyc, respectively having the cleavage maps of FIGS. 2 to 6, are transformed. These vectors may be introduced in a predetermined order or simultaneously. As mentioned above, respective exogenous promoters may be located upstream of the initiation codon of the genes.
  • the microorganism anchors at least one additional respective copy of aspB, lysC, asd, dap A, dapB, lysA and pycin the genomic DNA thereof.
  • a potent exogenous promoter is inserted between an initiation codon and an endogenous promoter for each gene.
  • the insertion of an exogenous gene into genomic DNA can be achieved using a method well known in the art, for example, homologous recombination.
  • Particularly useful in the present invention is Corynebacterium glutamicum KFCC-
  • This strain can be derived from Corynebacterium glutamicum KFCC- 10881 by introducing pDZ-2aspB, pDZ-2 lysC/ asd, pDZ-2dapA/dapB and pDZ-21ysA, respectively having the cleavagemaps of FIGS.
  • This strain can produce L-lysine at higher efficiency than the mother strain.
  • the L-lysine production efficiency can be further increased by the additional introduction of the vector pDZ-2pyc, having the cleavage map of FIG. 6, into the transformed strain so as to anchor two copies of pyc in the genomic DNA.
  • the present invention provides a method of producing L-lysine at a high yield, comprising the insertion of an exogenous promoter between a native promoter and an initiation codon for individual genes.
  • the promoters of the lysine biosynthesis genes are replaced with respective exogenous potent CJ7 promoters.
  • the CJ7 promoter useful in the present invention is a potent promoter, having the nucleotide sequence of SEQ ID NO. 44, derived from Corynebacterium ammoniagenes, which was previously developed by the present applicant (Korean Pat. No. KR-0620092).
  • the CJ7 promoter was found to increase the activity of aspartate kinase twice as much as the endogenous promoter.
  • CJ7 promoter Although only examples with the CJ7 promoter are given herein, it should be understood that the CJl to CJ6 promoters, disclosed in Korean Pat. No. KR- 0620092, respectively having nucleotide sequences of SEQ ID NOS.: 45 to 50 derived from Corynebacterium ammoniagenes, can be applied to the preparation of lysine- producing strains in the same manner as that used for the CJ7 promoter. Accordingly, the CJl to CJ6 promoters, as well as the CJ7 promoter, fall within the range of the exogenous promoter useful for increasing the expression level of genes of interest in accordance with the present invention.
  • the present invention provides a method for producing L-lysine, comprising:
  • the microorganism in the L-lysine production method according to the present invention is as described hereinbefore.
  • the Corynebacteria strain can be cultured in a batch process or a continuous process, such as a fed batch process or a repeated fed batch process.
  • Examples of carbon sources useful for culturing include saccharides and carbohydrates, such as glucose, saccharose, lactose, fructose, maltose, starch, cellulose and the like, oils and lipids, such as soybean oil, sunflower oil, castor oil, coconut oil and the like, fatty acids such as palmitic acid, stearic acid, linoleic acid and the like, alcohols such as glycerols, ethanol and the like, and organic acids such as acetic acid. These materials may be used alone or in combination.
  • saccharides and carbohydrates such as glucose, saccharose, lactose, fructose, maltose, starch, cellulose and the like
  • oils and lipids such as soybean oil, sunflower oil, castor oil, coconut oil and the like
  • fatty acids such as palmitic acid, stearic acid, linoleic acid and the like
  • alcohols such as glycerols, ethanol and the like
  • organic acids such as acetic
  • the nitrogen source useful in the culture medium for the bacteria of the present invention may be represented by peptone, yeast extract, broth, malt extract, a corn steep solid, soybean flour, urea, and inorganic compounds such as ammonium sulfate, ammonium chloride, ammonium phosphate, ammonium carbonate and ammonium nitrate. These nitrogen sources may be used alone or in combination. Potassium dihydrogen phosphate or dipotassium hydrogen phosphate or sodium salts thereof can be used as a nitrogen source in the culture medium. Also, the culture medium requires a metal salt, such as magnesium sulfate or iron sulfate, as an essential ingredient for the growth of the microorganism. In addition, other essential ingredients, such as amino acids and vitamins, are contained in the culture medium. Instead of the ingredients themselves, their precursors may be used. The ingredients may be added to a culture of the microorganism in a batch manner or a continuous manner.
  • the pH of the culture may be adjusted with a basic compound such as sodium hydroxide, potassium hydroxide or ammonia, or an acidic compound such as phosphoric acid or sulfuric acid.
  • a defoaming agent such as fatty acid poly glycol ester may be added to prevent the formation of bubbles.
  • An aerobic state may be maintained by injecting oxygen or oxygen-containing gas (e.g., air) into the culture. While the organism is cultured, the culture medium is maintained within the range from 20 to 45 0 C and preferably within the range from 25 to 4O 0 C. The culturing is continued until the production of L- amino acid reaches the maximum. In this regard, it takes 10 to 160 hours to attain the maximal amount of L- lysine. This amino acid may be released into the culture medium or may remain within the cells.
  • the recovering step is carried out as follows.
  • the recovery of L-lysine from cells or culture media is well known in the art.
  • Examples of L-lysine recovery methods include, but are not limited to, filtration, anion exchange chromatography, crystallization and HPLC.
  • Corynebacteria microorganisms of the present invention can produce L- lysine at higher yield.
  • FIG. 1 is a schematic view showing a vector pDZ for a nuclear-targeted gene into
  • FIG. 2 is a schematic view showing a vector pDZ-2aspB for a nuclear-targeted gene into Corynebacterium.
  • FIG. 3 is a schematic view showing a vector pDZ-21ysC/asd for a nuclear-targeted gene into Corynebacterium.
  • FIG. 4 is a schematic view showing a vector pDZ-2dapA/dapB for a nuclear- targeted gene into Corynebacterium.
  • FIG. 5 is a schematic view showing a vector pDZ-21ysA for a nuclear-targeted gene into Corynebacterium.
  • FIG. 6 is a schematic view showing a vector pDZ-2pyc for a nuclear-targeted gene into Corynebacterium.
  • FIG. 7 is a schematic view showing a vector pDZ-PCJ7.
  • FIG. 8 is a schematic view showing a vector pDZ-PCJ7/aspB.
  • FIG. 9 is a schematic view showing a vector pDZ-PCJ7/lysC.
  • FIG. 10 is a schematic view showing a vector pDZ-PCJ7/dapA.
  • FIG. 11 is a schematic view showing a vector pDZ-PCJ7/dapB.
  • FIG. 12 is a schematic view showing a vector pDZ-PCJ7/lysA.
  • FIG. 13 is a schematic view showing a vector pDZ-PCJ7/pyc.
  • GenBank accession # X06402 GenBank accession # X06402
  • a recombinant vector pDZ for carrying a Corynebacterium chromosome was constructed as follows.
  • a digest of a pACYClW vector resulting from treatment with Acul and Banl restriction enzymes was blunt-ended using a Klenow enzyme.
  • a lacZ gene from E. coli was prepared by gene amplification from the nuclear DNA of E. coli K12 W3110 through PCR, designed to contain the promoter thereof, and then by 5' end phosphorylation and blunt end generation with T4 DNA polymerase and polynucleotide kinase.
  • FIG. 1 is a schematic view showing the map of the vector pDZ for nuclear-targeted gene into Corynebacterium.
  • Corynebacterium glutamicum KFCC1O881, an L- lysine-producing strain, was transformed with the pDZ vector carrying two copies of a gene of interest in tandem by electroporation (using an electrical pulse method according to Appl. Microbiol. Biotechnol. (1999) 52:541-545) and screened for transformants,in which the gene of interest was inserted into the chromosome due to homology on a selection medium containing 25 mg/L of kanamycin. The appearance of a blue color on the solid medium containing X-gal
  • a strain into which the genes responsible for the pathway of lysine biosynthesis were to be inserted was based on Corynebacterium glutamicum (KFCC- 10881), which is resistant to S-(2-aminoethyl) cysteine (hereinafter referred to as "AEC”) and is homoserine-leaky.
  • KFCC- 10881 Corynebacterium glutamicum
  • AEC S-(2-aminoethyl) cysteine
  • the mutant strain KFCC- 10881 was prepared from the wild-type Corynebacterium glutamicum (ATCC 13032). A medium containing the mother strain at a concentration of 10 - 10 cells/ml was treated with 500 ⁇ g/ml of the mutagen N- methyl-N'-nitro-N-nitrosoguanidine (hereinafter referred to as "NTG") at 3O 0 C for 30 min, followed by the selection of colonies grown on a complex plate containing 5 g/1 of AEC. After the primary mutant strain was analyzed for ACE resistance and lysine productivity, it was led to secondary mutation with NTG.
  • NTG mutagen N- methyl-N'-nitro-N-nitrosoguanidine
  • a plurality of the colonies thus formed were tooth-picked into minimal media, which were or were not supplemented with homoserine so as to separate homoserine auxotrophs (secondary mutants), which cannot grow in a minimal medium lacking homoserine.
  • the homoserine auxotroph was allowed to undergo tertiary mutation so as to create a homoserine-leaky strain which was identified by incubation in a minimal medium containing 10 mg/L of homoserine.
  • the strain grown in the medium was examined for lysine productivity (Table 1).
  • the resulting lysine-producing strain which is AEC resistant and homoserine-leaky, was deposited with the Korean Federation of Culture Collection under the accession number of KFCC- 10881.
  • the minimal medium and the production medium used in this example are as follows.
  • EXAMPLE 3 Cloning of Lvsine-Producing Corvnebacterium ⁇ utamicum KFCC-10881-Derived aspB Gene. Construction of Recombinant Vector (pDZ-2aspB) and Preparation of Strain Anchoring aspB
  • PCR was performed on the aspB gene involved in the pathway of lysine biosynthesis, with the nuclear DNA of the lysine-producing PCR Coryneb ⁇ cterium glut ⁇ micum KFCC1O881 prepared in Example 2 serving as a template.
  • Information on the base sequence (NCBI Registration No. NC_003450, NcglO237) of the aspB gene was acquired from the data of the NIH GenBank and was used to design two pairs of primers to amplify an aspB gene ranging from the promoter region to the terminator codon (Table 2).
  • PCR was performed using the nuclear DNA of Corynebacterium glutamicum KFCC 10881 as a template and a set of oligonucleotide SEQ ID NOS. 1 and 2 or oligonucleotide SEQ ID NOS. 3 and 4 as primers in the presence of PfuUltra High- Fidelity DNA Polymerase (Stratagene), with 30 cycles of denaturing at 96 0 C for 30 sec, annealing at 53 0 C for 30 sec, and extending at 72 0 C for 2min.
  • PfuUltra High- Fidelity DNA Polymerase (Stratagene)
  • the PCR products thus obtained were found to be two kinds of aspB genes (aspB-A and aspB-B), each containing a l,493bp-long promoter region, which were produced respectively with a set of SEQ ID NOS. 1 and 2 and a set of SEQ ID NOS. 3 and 4.
  • the PCR products were cloned into the E. coli vector pCR2.1 with the aid of a TOPO Cloning Kit (Invitrogen) to give recombinant vectors pCR-aspB-A and pCR-aspB-B.
  • FIG. 2 is a map of a pDZ-2aspB vector for a nuclear-targeted gene into Corynebacterium.
  • EXAMPLE 4 Cloning of Lysine-Producing Corvnebacterium glutamicum KFCC-10881-Derived lvsC/asd Gene. Construction of Recombinant Vector (pDZ-21ysC/asd) and Preparation of Strain Anchoring lysC/asd
  • PCR was performed using the nuclear DNA of Coryneb ⁇ cterium glutamicum KFCC 10881 as a template and aset of oligonucleotide SEQ ID NOS. 1 and 2 or oligonucleotide SEQ ID NOS. 3 and 4 as primers in the presence of PfuUltra High- Fidelity DNA Polymerase (Stratagene), with 30 cycles of denaturing at 96 0 C for 30 sec, annealing at 52 0 C for 30 sec, and extending at 72 0 C for 3 min.
  • PfuUltra High- Fidelity DNA Polymerase (Stratagene)
  • the PCR products thus obtained were found to be two kinds of lysC/asd genes, lysC/asd-A and lysC/asd-B, each containing a 2,805bp-long promoter region, which were produced respectively with a set of SEQ ID NOS. 5 and 6 and a set of SEQ ID NOS. 7 and 8.
  • the PCR products were cloned into the E. coli vector pCR2.1 with the aid of a TOPO Cloning Kit (Invitrogen) to give recombinant vectors pCR-lysC/asd-A and pCR-lysC/asd-B.
  • FIG. 3 is a map of the pDZ-21ysC/asd vector for a nuclear- targeted gene into Corynebacterium.
  • EXAMPLE 5 Cloning of Lvsine-Producing Corvnebacterium ⁇ utamicum KFCC-10881-Derived dapA/dapB Gene. Construction of Recombinant Vector (pDZ-2dapA/dapB) and Preparation of Strain Anchoring dapA/dapB
  • PCR was performed using the nuclear DNA of Corynebacterium glutamicum KFCC 10881 as a template and a set of oligonucleotide SEQ ID NOS. 9 and 10 or oligonucleotide SEQ ID NOS. 11 and 12 as primers in the presence of PfuUltra High-Fidelity DNA Polymerase (Stratagene), with 30 cycles of denaturing at 96 0 C for 30 sec, annealing at 52 0 C for 30 sec and extending at 72 0 C for 3 min.
  • PfuUltra High-Fidelity DNA Polymerase (Stratagene)
  • the PCR products thus obtained were found to be two kindsof dapA/dapB genes, dapA/dapB-A, dapA/dapB-B, each containing a 3,210bp-long promoter region, which were produced respectively with a set of SEQ ID NOS. 9 and 10 and a set of SEQ ID NOS. 11 and 12.
  • the PCR products were cloned into the E. coli vector pCR2.1 with the aid of the TOPO Cloning Kit (Invitrogen) to give recombinant vectors pCR- dapA/dapB-A and pCR-dapA/dapB-B.
  • FIG. 4 is a map of the pDZ- 2dapA/dapB vector.
  • the recombinant vector pDZ-2dapA/dapB was transformed into the lysine- producing Corynebacterium glutamicum KFCC10881-CJ2 prepared in Example 4, followed by the insertion of an additional copy of dapA/dapB gene just next to the dapA/dapB gene in the nuclear DNA through crossover so as to produce a lysine- producing strain anchoring two copies of the dapA/dapB gene, which was named Corynebacterium glutamicum KFCC10881-CJ3.
  • the adjacent positioning of two copies of dapA/dapB gene was identified by PCR using a set of primers (Table 7) designed to amplify a contact region between the two copies of dapA/dapB gene.
  • Ncgll 132-1133 of lysA gene was acquired from data of the NIH GenBank.
  • the lysA gene was analyzed to comprise an argS gene (arginyl-tRNA synthetase) and an operon. The information was used to design two pairs of primers to amplify the overall argS- lysA gene ranging from the argS promoter to the terminator codon (Table 8).
  • PCR was performed using the nuclear DNA of Corynebacterium glutamicum KFCC 10881 as a template and a set of oligonucleotide SEQ ID NOS. 13 and 14 or SEQ ID NOS. 15 and 16 as primers in the presence of PfuUltraTM High-Fidelity DNA Polymerase (Stratagene), with 30 cycles of denaturing at 96 0 C for 30 sec, annealing at 52 0 C for 30 sec and extending at 72 0 C for 4 min.
  • PfuUltraTM High-Fidelity DNA Polymerase (Stratagene)
  • the PCR products thus obtained were found to be two kinds of argS/lysA genes, argS/lysA-A and argS/lysA-B, each containing a 3,359bp-long promoter region, which were produced respectively with a set of SEQ ID NOS. 13 and 14 and a set of SEQ ID NOS. 15 and 16.
  • the PCR products were cloned into the E. coli vector pCR2.1 with the aid of a TOPO Cloning Kit (Invitrogen) to give recombinant vectors pCR- argS/lysA-A and pCR-argS/lysA-B.
  • FIG. 5 is a map of the pDZ-21ysA vector.
  • the recombinant vector pDZ-21ysA was transformed into the lysine-producing Corynebacterium glutamicum KFCC10881-CJ3 prepared in Example 5, followed by the insertion of an additional copy of lysA gene just next to the lysA gene in the nuclear DNA through crossover so as to produce a lysine-producing strain anchoring two copies of lysA gene, which was named Corynebacterium glutamicum KFCC 10881 -C J4.
  • the adjacent positioning of two copies of lysA gene was determined through PCR using a set of primers (Table 9) designed to amplify a contact region between the two copies of lysA gene.
  • EXAMPLE 7 Cloning of Lysine-Producing Corynebacterium glutamicum KFCC-10881-Derived pycGene. Construction of Recombinant Vector (pDZ-2pyc) and Preparation of Strain Anchoring pvc
  • PCR was performed using the nuclear DNA of Corynebacterium glutamicum KFCC 10881 as a template and a set of oligonucleotide SEQ ID NOS. 31 and 32 or SEQ ID NOS. 33 and 34 as primers in the presence of PfuUltraTM High-Fidelity DNA Polymerase (Stratagene), with 30 cycles of denaturing at 96 0 C for 30 sec, annealing at 52 0 C for 30 sec, and extending at 72 0 C for 4 min.
  • PfuUltraTM High-Fidelity DNA Polymerase (Stratagene)
  • the PCR products thus obtained were found to be two kinds of pyc genes, pyc- A and pyc-B, each containing a 3,925bp-long promoter region, which were produced respectively with a set of SEQ ID NOS. 31 and 32 and a set of SEQ ID NOS. 33 and 34.
  • the PCR products were cloned into the E. coli vector pCR2.1 with the aid of a TOPO Cloning Kit (Invitrogen) to give recombinant vectors pCR-pyc-A and pCR-pyc-B.
  • FIG. 6 is a map of the pDZ-2pyc vector.
  • Corynebacterium glutamicum KFCC10881-CJ4 prepared in Example 6, followed by the insertion of an additional copy of pycA gene just next to the pycA gene in the nuclear DNA through crossover so as to produce a lysine-producing strain anchoring two copies of pyc gene, which was named Corynebacterium glutamicum KFCC 10881 -C J5.
  • the adjacent positioning of two copies of pyc gene was determined through PCR using a set of primers (Table 11) designed to amplify the contact region between the two copies of pyc gene.
  • KFCC 10881 -C J5 anchors the seven genes involved in lysine biosynthesis.
  • EXAMPLE 8 Production of Lysine from Strains Anchoring Genes Re- sponsible for Lysine-Biosynthesis
  • 10881-CJ5 were inoculated into 240 ml-corner baffle flasks containing 25 ml of the following seed medium and cultured at 3O 0 C for 20 hour with shaking at 200 rpm.
  • the seed medium and the production medium comprise the following compositions.
  • [117] Seed medium TPH 7.0)
  • [119] Glucose 20 g, peptone 10 g, yeast extract 5 g, urea 1.5 g, KH PO 4 g, K HPO 8 g, MgSO 7H O 0.5 g, biotin 100 D, thiamine HCl 1000 D, calcium pantothenate 2000 D,
  • Corynebacterium glutamicum KFCC- 10881 -C J4 in which the six genes involved in lysine biosynthesis are anchored, was found to increase in lysine productivity by about 7%, compared with the mother strain KFCC- 10881. Also, it was measured that an increase of about 8% in lysine production was obtained with Corynebacterium glutamicum KFCC- 10881 -C J5, which anchors a pyc gene in addition to the six lysine biosynthesis genes, in comparison to the mother strain KFCC- 10881.
  • the seed medium and the production medium comprise the following compositions.
  • EXAMPLE 12 Construction of Vector for Promoter Replacement and Preparation of Strain Replaced Exogenous Promoter for Lysine Biosynthesis Gene
  • the CJ7 promoter is a strong, Corynebacterium ammoniagenes-de ⁇ ved promoter having a base sequence represented by SEQ ID NOS. 44 to 50. It is disclosed in Korean Pat. No. 0620092, issued to the present applicant.
  • SEQ ID NOS. 44 to 50 SEQ ID NOS. 44 to 50.
  • a vector for introducing the CJ7 promoter into the nuclear DNA of the lysine- producing strains was prepared as follows.
  • a pDZ vector was treated with restriction enzymes Xbal and Ndel. PCR was performed in the presence of SEQ ID NOS. 42 and 43 (Table 17) as primers designed to insert Xbal and Ndel sites respectively at the 5'- and the 3 '-end of a PCR product amplified from the CJ7 promoter of the nuclear DNA of Corynebacterium am- moniagenes. After treatment with Xbal and Ndel, the CJ7 promoter PCR product was ligated to the truncated pDZ vector to give a pDZ-PCJ7 vector, which served as a primary plasmid for introducing a CJ7 promoter into the nuclear DNA of the strain (FIG. 7)
  • the primers used forthe PCR were designed such that an Xbal site was inserted at opposite ends of the PCR product of the partial native promoter fragment and an Ndel site was inserted at opposite ends of the PCR product of the partial ORF. These PCR products were treated with respective restriction enzymes.
  • pDZ-PCJ7 was digested with Xbal for ligation to the truncated PCR product of the partial native promoter fragment and then with Ndel for ligation to the truncated PCR production of the partial ORF to construct recombinant plasmids, respectively named pDZ-PCJ7-aspB, pDZ-PCJ7-lysCasd, pDZ- PCJ7-dapA, pDZ-PCJ7-dapB, pDZ-PCJ7-argSlysA and pDZ-PCJ7-pyc, each comprising a CJ7 promoter located between the two PCR DNA fragments (FIGS. 8 to 13).
  • the plasmids were used for the recombination of target genes as follows. First, the recombinant vector pDZ-PCJ7-aspB was transformed into the lysine-producing Corynebacterium glutamicum KFCC- 10881, which then underwent crossover to the CJ7 promoter at the promoter region of the aspB gene inthe nuclear DNA. In the same way, the other recombinant plasmids were transformed in order to create a novel strain KFCC-10881-PCJ7-5 in which a CJ7 promoter is located at the promoter regions of aspB, lysCasd, dapA, dapB and argSlysA genes. In addition to the promoters, the promoter of the pyc gene was substituted with a CJ7 promoter to create KFCC- 10881-PCJ7-6.
  • 10881-PCJ7-6 were inoculated into 250 ml-corner baffle flasks containing 25 ml of the following seed medium, and were cultured at 3O 0 C for 20 hours with shaking at 200 rpm. Thereafter, 1 ml of each of the cultures was inoculated into a 250 ml-corner baffle flask containing 24 ml of the following production medium and cultured at 3O 0 C for 120 hours with shaking at 200 rpm.
  • the seed medium and the production medium comprise the following compositions.
  • Corynebacterium glutamicum KFCC- 10881-PCJ7-5 in which the six genes involved in lysine biosynthesis were anchored along with respective exogenous CJ7 promoters therefor and Corynebacterium glutamicum KFCC- 10881-PCJ7-6, in which a pyc gene and a CJ7 promoter therefor were anchored in addition to the six genes and promoters, were found to increase in lysine productivity by about 17.4% and 18.6% respectively, compared with the mother strain KFCC- 10881.
  • EXAMPLE 14 Activity of Lysine Biosynthesis Enzymes in Strain Anchoring Additional Gene Responsible for Lysine Biosynthesis and Having Replaced Exogenous Promoter therefor
  • the modified lysine-producing strains were found to increase in enzyme activity compared to the initial mother strain KFCC 10881 (Table 19) as measured by the method according to Pechere J. F. and Capony J. P. (Anal Biochem 22: 536-539, 1968) for aspartate kinase activity and the method according to J. Cremer et al. for diaminopimelate dicarboxylase activity.

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Abstract

L'invention concerne une variante de Corynebacterium qui présente une activité supérieure à l'activité endogène aspartate aminotransférase, aspartate kinase, aspartate semialdéhyde déshydrogénase, dihydrodipicolinate synthase, dihydropicolinate réductase, et diaminopimélate dicarboxylase, et éventuellement pyruvate carboxylase. L'invention concerne également un procédé de production de la L-lysine grâce à l'utilisation de ladite variante.
PCT/KR2007/004478 2006-09-15 2007-09-17 Bactéries coryneformes présentant une productivité de l-lysine améliorée et procédé de production de l-lysine associé Ceased WO2008033001A1 (fr)

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BRPI0716980-9A2A BRPI0716980A2 (pt) 2006-09-15 2007-09-17 Corynebacteria com produtividade de l-lisina aumentada e método de produção da l-lisina usando a mesma
JP2009528183A JP5756259B2 (ja) 2006-09-15 2007-09-17 Ｌ−リジン生産能の向上したコリネバクテリウム属およびそれを用いたｌ−リジン生産方法
EP07808268A EP2066782A4 (fr) 2006-09-15 2007-09-17 Bacteries coryneformes presentant une productivite de l-lysine amelioree et procede de production de l-lysine associe
CN2007800341803A CN101573438B (zh) 2006-09-15 2007-09-17 具有增加的l-赖氨酸生产力的棒状杆菌和使用其生产l-赖氨酸的方法
AU2007295159A AU2007295159B2 (en) 2006-09-15 2007-09-17 A Corynebacteria having enhanced L-lysine productivity and a method of producing L-lysine using the same
US12/441,358 US9109242B2 (en) 2006-09-15 2007-09-17 Corynebacteria having enhanced L-lysine productivity and a method of producing L-lysine using the same

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JP6695308B2 (ja) 2020-05-20
JP5756259B2 (ja) 2015-07-29
US20100143984A1 (en) 2010-06-10
EP2066782A4 (fr) 2010-02-03
US9109242B2 (en) 2015-08-18
BRPI0716980A2 (pt) 2013-10-22
AU2007295159A1 (en) 2008-03-20
EP2066782A1 (fr) 2009-06-10
KR20080025355A (ko) 2008-03-20
JP2017221202A (ja) 2017-12-21
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